STERITEC DISPOSABLE BIOLOGICAL TEST PACK— 510(k) K961721
Substantially EquivalentSteritec Products Mfg Co, Inc.
FDA 510(k) clearance K961721 for STERITEC DISPOSABLE BIOLOGICAL TEST PACK, Substantially Equivalent on 1996-08-23. Applicant: Steritec Products Mfg Co, Inc.. Device class: 2.
Clearance details
- Applicant
- Steritec Products Mfg Co, Inc.
- Product code
- Code FRC
- Device class
- Class 2
- Regulation
- 21 CFR 880.2800
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Castle Rock, CO, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.